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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098925copy number variation1nstd102humanPathogenic GRCh38 chr19: 15,014,099-16,261,691 , GRCh37.p13 chr19: 15,124,911-16,372,502 CYP4F12, OR1AB1P, 52 more genes
    nsv7095645copy number variation1nstd102humanUncertain significance GRCh37 chr19: 14,847,048-17,394,124 , GRCh38.p12 chr19: 14,736,236-17,283,315 HAUS8, MIR1470, 95 more genes
    nsv7075473inversion1nstd229human GRCh38 chr19: 12,694,752-17,614,167 , GRCh37.p13 chr19: 12,805,566-17,724,976 SYDE1, LOC107985287, 207 more genes
    nsv7065580inversion1nstd229human GRCh38 chr19: 11,963,576-20,150,892 , GRCh37.p13 chr19: 12,074,391-20,193,556 CYP4F24P, CYP4F2, 359 more genes
    nsv7065429inversion1nstd229human GRCh38 chr19: 16,102,064-16,102,536 , GRCh37.p13 chr19: 16,212,874-16,213,346 TPM4
    nsv7063135inversion1nstd229human GRCh38 chr19: 12,625,698-17,530,884 , GRCh37.p13 chr19: 12,736,512-17,641,693 SYCE2, OR1AB1P, 212 more genes
    nsv7060542inversion1nstd229human GRCh38 chr19: 12,342,956-19,691,233 , GRCh37.p13 chr19: 12,453,770-19,802,042 DDX39A, KCNN1, 314 more genes
    nsv7059139inversion1nstd229human GRCh38 chr19: 12,641,624-19,910,103 , GRCh37.p13 chr19: 12,752,438-20,020,912 NR2F6, ISCA1P5, 307 more genes
    nsv7017356copy number variation1nstd229human GRCh38 chr19: 16,094,891-16,098,529 , GRCh37.p13 chr19: 16,205,701-16,209,339 TPM4
    nsv6999434copy number variation1nstd229human GRCh38 chr19: 16,090,854-16,090,982 , GRCh37.p13 chr19: 16,201,664-16,201,792 TPM4
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6523599copy number variation1nstd223human GRCh38 chr19: 16,069,427-16,069,620 , GRCh37.p13 chr19: 16,180,237-16,180,430 TPM4
    nsv6523147copy number variation1nstd223human GRCh38 chr19: 16,075,055-16,079,283 , GRCh37.p13 chr19: 16,185,865-16,190,093 TPM4
    nsv6287915insertion2nstd214human GRCh38 chr19: 16,069,538-16,069,538 , GRCh37.p13 chr19: 16,180,348-16,180,348 TPM4
    nsv6242817mobile element insertion1nstd215human GRCh38 chr19: 16,075,538-16,075,538 , GRCh37.p13 chr19: 16,186,348-16,186,348 TPM4
    nsv6242815mobile element insertion1nstd215human GRCh38 chr19: 16,073,179-16,073,179 , GRCh37.p13 chr19: 16,183,989-16,183,989 TPM4
    nsv6145726copy number variation1nstd206human GRCh38 chr19: 16,069,363-16,069,756 , GRCh37.p13 chr19: 16,180,173-16,180,566 TPM4
    nsv6133691copy number variation1nstd213human GRCh37 chr19: 15,360,000-18,450,001 , GRCh38.p12 chr19: 15,249,189-18,339,191 BST2, NR2F6, 123 more genes
    nsv6133690copy number variation1nstd213human GRCh37 chr19: 13,260,000-16,840,001 , GRCh38.p12 chr19: 13,149,186-16,729,190 PRKACA, SLC1A6, 137 more genes
    nsv6129689insertion1nstd186human GRCh37 chr19: 16,180,348-16,180,399 , GRCh38.p12 chr19: 16,069,538-16,069,589 TPM4
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